FDA Inspection 575622 — Sumbaker GP

Sumbaker GP — FEI 3004109642

The FDA completed an inspection of Sumbaker GP on April 3, 2009 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 3, 2009
Fiscal Year
2009
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Memphis, TN (United States)